Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×

  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.



  • Celiac.com Sponsor (A1):

    Celiac.com Sponsor (A1-M):

  • Get Celiac.com Updates:
    Support Celiac.com!
    eNewsletter
    Donate

New Haven, Ct Area?

MaddyK

By MaddyK
in Meet Up Room

Recommended Posts

MaddyK Newbie
MaddyK
Posted

Any other young adults in the New Haven CT area that would be interested in getting together with another recently diagnosed PhD student for support and doing fun things that are 'celiac friendly'?

Link to comment
Share on other sites
Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):

Celiac.com Sponsor (A8-M):


AndrewNYC Explorer
AndrewNYC
Posted

Maybe. Would be a roadtrip. E-mail me on the board if you'd like to discuss. I'm probably near your age.

Any other young adults in the New Haven CT area that would be interested in getting together with another recently diagnosed PhD student for support and doing fun things that are 'celiac friendly'?
Link to comment
Share on other sites
chriscal2 Newbie
chriscal2
Posted
Maybe. Would be a roadtrip. E-mail me on the board if you'd like to discuss. I'm probably near your age.

I go to school in Fairfield and I'm living up here for the summer. Know any details yet?

Link to comment
Share on other sites
  • 4 weeks later...
ndshiffrin Newbie
ndshiffrin
Posted
Any other young adults in the New Haven CT area that would be interested in getting together with another recently diagnosed PhD student for support and doing fun things that are 'celiac friendly'?

Hi! I'm moving to New Haven to start a Ph.D. next month and I would love to meet up to find some celiac friendly restaurants or cook.

Link to comment
Share on other sites
  • 2 weeks later...
Sinenox Apprentice
Sinenox
Posted

Hello. I have just moved in to New Haven to start a PhD as well. I have found the local restaurants sorely lacking, unfortunately. I would love to get together with other local celiacs (particularly other grad students) to cook and discuss. Let me know when you get into town. I would be happy to help to organize something a little more formal as well, if you're interested.

Link to comment
Share on other sites
babysteps Contributor
babysteps
Posted

In New Haven, Foster's is pretty accommodating (they will even do gluten-free birthday cake with advance warning), but there are knowledge gaps, last time we were there no one seemed to realize miso often (or perhaps always, depending on your view & the source of info) contains gluten.

Ibiza did a great job with warning when I was part of a group meal there this spring. They seem very aware of food issues, someone else at our table had a shellfish allergy but didn't realize until he sat down that it was an issue with the night's menu, they were able to make him a substitute course on the fly.

Cafe Istanbul- I ate cleanly there at a drop-in meal. The waitperson wasn't familiar with celiac but picked up very quickly & I felt comfortable.

A recent (July 30) post on Open Original Shared Link said Clair's Corner Copia has a gluten-free menu.

Happy eating! I am semi-close by, in Fairfield.

Link to comment
Share on other sites
  • 1 month later...
belle-44 Newbie
belle-44
Posted
Any other young adults in the New Haven CT area that would be interested in getting together with another recently diagnosed PhD student for support and doing fun things that are 'celiac friendly'?

I just moved to New Haven for grad school as well, and was diagnosed about a week before I moved here. Any out there willing to pass along info/meet to chat about living and eating gluten free?

Link to comment
Share on other sites
Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):

Celiac.com Sponsor (A8-M):


  • 1 month later...
luciddream928 Explorer
luciddream928
Posted

Hi,

I'm originally from New Haven, and I know that there is a new place called Nature's Grocer that has a dedicated gluten-free bakery. Their website is: Open Original Shared Link

Also, "Edge of the Woods" (if they are still around, on State St. I believe) might have a very good selection of gluten-free products.

There is a Trader Joe's in Orange and a Whole Foods further north, but the WF would be about a 45 min. drive. I think it's in West Hartford.

Blessings,

Rachel

Link to comment
Share on other sites

Archived

This topic is now archived and is closed to further replies.

Go to topic listing
  • Celiac.com Sponsor (A19):


  • Member Statistics

    • Total Members
      121,074
    • Most Online (within 30 mins)
      7,748
    Robert Noah
    Newest Member
    Robert Noah
    Joined
  • Celiac.com Sponsor (A20):

  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m
  • Celiac.com Sponsor (A22):



  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Nacina
      14 year old with Celiac & EOE still suffering...

      By Nacina · Posted

      Well, that's a big question. When he was seeing the nutrition response testing dr. that changed each time we went in. He hasn't been seeing him regularly for theist ten months. When he had a horribly week in March I started him back on the 4 that were suggested to keep him on. Those are: Standard Process Chlorophyll Complex gluten-free, SP A-F Betafood gluten-free, SP Tuna Omega-3 Oil gluten-free, And Advanced Amino Formula. He also takes a one a day from a company called Forvia (multivitamin and mineral) and Probiotic . Recently he had to start Vitamin D as well as he was deficient.  
    • Fluka66
      Waiting for urgent referral.

      By Fluka66 · Posted

      Thank you again for your reply and comments which I have read carefully as I appreciate any input at this stage. I'm tending to listen to what my body wants me to do, having been in agony for many years any respite has been welcome and avoiding all wheat and lactose has thankfully brought this.  When in pain before I was seen by a number of gynacologists as I had 22 fibroids and had an operation 13 years ago to shrink them . However the pain remained and intensified to the point over the years where I began passing out. I was in and out of a&e during covid when waiting rooms where empty. My present diet is the only thing that's given me any hope for the future. As I say I had never heard of celiac disease before starting so I guess had this not come up in a conversation I would just have carried on. It was the swollen lymph node that sent me to a boots pharmacist who immediately sent me to a&e where a Dr asked questions prescribed antibiotics and then back to my GP. I'm now waiting for my hospital appointment . Hope this answers your question. I found out more about the disease because I googled something I wouldn't normally do, it did shed light on the disease but I also read some things that this disease can do. On good days I actually hope I haven't got this but on further investigation my mother's side of the family all Celtic have had various problems 're stomach pain my poor grandmother cried in pain as did her sister whilst two of her brother's survived WW2 but died from ulcers put down to stress of fighting.  Wishing you well with your recovery.  Many thanks  
    • knitty kitty
      14 year old with Celiac & EOE still suffering...

      By knitty kitty · Posted

      Welcome to the forum, @Nacina, What supplements is your son taking?
    • knitty kitty
      This forum might be the last hope I have in my life. Please I beg you

      By knitty kitty · Posted

      @BluegrassCeliac, I'm agreeing.  It's a good thing taking magnesium. And B vitamins. Magnesium and Thiamine work together.  If you supplement the B vitamins which include Thiamine, but don't have sufficient magnesium, Thiamine won't work well.  If you take Magnesium, but not Thiamine, magnesium won't work as well by itself. Hydrochlorothiazide HCTZ is a sulfonamide drug, a sulfa drug.  So are proton pump inhibitors PPIs, and SSRIs. High dose Thiamine is used to resolve cytokine storms.  High dose Thiamine was used in patients having cytokine storms in Covid infections.  Magnesium supplementation also improves cytokine storms, and was also used during Covid. How's your Vitamin D? References: Thiamine and magnesium deficiencies: keys to disease https://pubmed.ncbi.nlm.nih.gov/25542071/ Hiding in Plain Sight: Modern Thiamine Deficiency https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533683/ The Effect of a High-Dose Vitamin B Multivitamin Supplement on the Relationship between Brain Metabolism and Blood Biomarkers of Oxidative Stress: A Randomized Control Trial https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316433/ High‐dose Vitamin B6 supplementation reduces anxiety and strengthens visual surround suppression https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787829/ Repurposing Treatment of Wernicke-Korsakoff Syndrome for Th-17 Cell Immune Storm Syndrome and Neurological Symptoms in COVID-19: Thiamine Efficacy and Safety, In-Vitro Evidence and Pharmacokinetic Profile https://pubmed.ncbi.nlm.nih.gov/33737877/ Higher Intake of Dietary Magnesium Is Inversely Associated With COVID-19 Severity and Symptoms in Hospitalized Patients: A Cross-Sectional Study https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132593/ Magnesium and Vitamin D Deficiency as a Potential Cause of Immune Dysfunction, Cytokine Storm and Disseminated Intravascular Coagulation in covid-19 patients https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861592/ Sulfonamide Hypersensitivity https://pubmed.ncbi.nlm.nih.gov/31495421/
    • BluegrassCeliac
      This forum might be the last hope I have in my life. Please I beg you

      By BluegrassCeliac · Posted

      Hi,   Not saying Thiamine (B1) couldn't be an issue as well, but Mg was definitely the cause of my problems. It's the only thing that worked. I supplemented with B vitamins, but that didn't change anything, in fact they made me sick. Mg stopped all my muscle pain (HCTZ) within a few months and fixed all the intestinal problems HCTZ caused as well. Mom has an allergy to some sulfa drugs (IgG Celiac too), but I don't think I've ever taken them. Mg boosted my energy as well. It solved a lot of problems. I take 1000mg MgO a day with no problems. I boost absorption with Vitamin D. Some people can't take MgO,  like mom, she takes Mg Glycinate. It's one of those things that someone has try and find the right form for themselves. Everyone's different. Mg deficiency can cause anxiety and is a treatment for it. A pharmacist gave me a list of drugs years ago that cause Mg deficiency: PPIs, H2 bockers, HCTZ, some beta blockers (metoprolol which I've taken -- horrible side effects), some anti-anxiety meds too were on it. I posted because I saw he was an IgG celiac. He's the first one I've seen in 20 years, other than my family. We're rare. All the celiacs I've met are IgA. Finding healthcare is a nightmare. Just trying to help. B  
×
×
  • Create New...